Injection Port Applier with Downward Force Actuation

ABSTRACT

An injection port applier is configured to engage an injection port that has integral fasteners that are movable from a non-deployed position to a deployed position. The applier comprises a shaft, a port engagement portion, and a handle. The port engagement portion is includes a fastener deployment member that is operable to move the fasteners to the deployed position. The handle comprises a first handle portion and a second handle portion. The second handle portion is movable distally relative to the first handle portion in order to actuate the fastener deployment member, to thereby move the fasteners to the deployed position. An elongate actuating member couples the second handle portion with the fastener deployment member. One part of the elongate actuating member translates longitudinally in response to the second handle being moved distally; while another part of the elongate actuating member rotates in response to the first portion translating.

This application is a continuation-in-part of U.S. patent application Ser. No. 11/166,625, filed Jun. 24, 2005, entitled “Implantable Medical Device with Reversible Attachment Mechanism and Method,” published as U.S. Pub. No. 2005/0283119, which is a continuation in part of U.S. patent application Ser. No. 10/741,875, filed Dec. 19, 2003, entitled “Subcutaneous Self Attaching Injection Port with Integral Moveable Retention Members,” published as U.S. Pub. No. 2004/0254537, which claims priority to U.S. Provisional Patent Application Ser. No. 60/478,763, filed Jun. 16, 2003, entitled “Fluid Injection Port for Adjustable Gastric Band.” The disclosure of each of those three patent applications is incorporated by reference herein.

This application also incorporates by reference the following U.S. patent applications, both of which were filed on Dec. 19, 2003: application Ser. No. 10/741,127, entitled “Subcutaneous Injection Port for Applied Fasteners,” published as U.S. Pub. No. 2005/0131352; and application Ser. No. 10/741,868, entitled “Subcutaneous Self Attaching Injection Port with Integral Fasteners,” issued as U.S. Pat. No. 7,374,557.

TECHNICAL FIELD

The present invention relates generally to medical implants and appliers therefor, and more particularly to an attachment mechanism for use with a variety of medical implants and appliers for attaching such medical implants to body tissue. The invention will be disclosed in connection with, but not limited to, surgically implantable injection ports and an applier therefor.

BACKGROUND

Implantable medical devices are typically implanted in a patient to perform a therapeutic function for that patient. Non-limiting examples of such devices include pace makers, vascular access ports, injection ports (such as used with gastric bands) and gastric pacing devices. Such implants need to be attached, typically subcutaneously, in an appropriate place in order to function properly. It is desirable that the procedure to implant such devices be quick, easy and efficient. In many instances it would be beneficial if the surgeon could remove or reposition the device quickly, easily and efficiently.

Injection ports are placed beneath the skin of a body for injecting fluids into the body, such as for infusing medication, blood draws, and many other applications, including adjustable gastric bands. Since the early 1980s, adjustable gastric bands have provided an effective alternative to gastric bypass and other irreversible surgical weight loss treatments for the morbidly obese. The gastric band is wrapped around an upper portion of the patient's stomach, forming a stoma that restricts food passing from an upper portion to a lower portion of the stomach. When the stoma is of the appropriate size, food held in the upper portion of the stomach provides a feeling of fullness that discourages overeating. However, initial maladjustment or a change in the stomach over time may lead to a stoma of an inappropriate size, warranting an adjustment of the gastric band. Otherwise, the patient may suffer vomiting attacks and discomfort when the stoma is too small to reasonably pass food. At the other extreme, the stoma may be too large and thus fail to slow food moving from the upper portion of the stomach, defeating the purpose altogether for the gastric band.

In addition to a latched position to set the outer diameter of the gastric band, adjustability of gastric bands is generally achieved with an inwardly directed inflatable balloon, similar to a blood pressure cuff, into which fluid, such as saline, is injected through a fluid injection port to achieve a desired diameter. Since adjustable gastric bands may remain in the patient for long periods of time, the fluid injection port is typically installed subcutaneously to avoid infection, for instance in front of the sternum. Adjusting the amount of fluid in the adjustable gastric band is achieved by inserting a Huber needle through the skin into a silicon septum of the injection port. Once the needle is removed, the septum seals against the hole by virtue of compressive load generated by the septum. A flexible conduit communicates between the injection port and the adjustable gastric band.

The present invention encompasses an attachment mechanism to secure an medical implant device to body tissue quickly and easily. The attachment mechanism may be reversible, allowing the implantable medical device to be detached quickly and easily for repositioning or removal. Although standard, commercially available instruments may be used to actuate the attachment mechanism, the present invention also encompasses an applier for locating an implantable medical device in the desired location and quickly and easily actuating the attachment mechanism to secure the implantable medical device.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the invention, and, together with the general description of the invention given above, and the detailed description of the embodiments given below, serve to explain the principles of the present invention.

FIG. 1 is a perspective view of an injection port with an attachment mechanism constructed in accordance with the present invention.

FIG. 2 is a top view of the injection port of FIG. 1.

FIG. 3 is a bottom view of the injection port of FIG. 1.

FIG. 4 is a cross sectional view of the injection port of FIG. 1 taken along line 4-4 of FIG. 3.

FIG. 5 is an exploded perspective view of the injection port of FIG. 1.

FIG. 6 is perspective view of the bottom of the injection port of FIG. 1, showing the attachment mechanism in the retracted position.

FIG. 7 is a perspective view of the bottom of the injection port of FIG. 1, similar to FIG. 6, showing the attachment mechanism in the extended/fired position.

FIG. 8 is a side cutaway view in partial cross-section illustrating a fastener of the attachment mechanism in the retracted position.

FIG. 9 is a side cutaway view in partial cross-section similar to FIG. 8 illustrating a fastener of the attachment mechanism that is being advanced by the actuator ring toward the extended/fired position.

FIG. 10 is a side cutaway view in partial cross-section similar to FIG. 8 illustrating a fastener of the attachment mechanism in the extended/fired position.

FIG. 11 is a side cutaway view in partial cross-section similar to FIG. 8 illustrating a fastener of the attachment mechanism that is being advanced by the actuator ring toward the retracted position.

FIG. 12 is a top view of the injection port of FIG. 1, with the actuator ring omitted to illustrate the positions of the links when the fasteners are in the retracted position.

FIG. 13 is a top view of the injection port of FIG. 1, with the actuator ring omitted to illustrate the positions of the links when the fasteners are in the extended/fired position.

FIG. 14 is an enlarged, fragmentary top view of the visual position indicator and actuator ring detent system of the attachment mechanism of FIG. 1, in the retracted position.

FIG. 15 is an enlarged, fragmentary top view of the visual position indicator and actuator ring detent system of the attachment mechanism of FIG. 1 in the extended/fired position.

FIG. 16 is an enlarged, fragmentary, exploded perspective view of the fitting and locking connector of the injection port of FIG. 1.

FIG. 17 is an enlarged, fragmentary partial cross-section view of the locking connector assembled to the fitting the septum retainer but not locked in place.

FIG. 18 is an enlarged, fragmentary partial cross-section view similar to FIG. 17 showing the locking connector locked in place.

FIG. 19 is an enlarged perspective view of the safety cap.

FIG. 20 is a perspective view of an applier constructed to implant the injection port of FIG. 1.

FIG. 21 is a exploded, perspective view of the applier of FIG. 20.

FIG. 22 is a side view of the applier of FIG. 20 with one of the two body halves showing the internal components in the unapplied, non-actuated position.

FIG. 23 is a side view of the applier of FIG. 20 similar to FIG. 22, showing the internal components in the applied, actuated position.

FIG. 24 is an enlarged, fragmentary side view of the linear to rotary cam mechanism of the applier of FIG. 20.

FIG. 25 is an enlarged top perspective view of the locator of the applier of FIG. 20.

FIG. 26 is an enlarged bottom perspective view of the locator and the port actuator of the applier of FIG. 20.

FIG. 27 is a partially cut away end view of the locator of the applier of FIG. 20.

FIG. 28 is an enlarged, cross sectional view of the injection port of FIG. 1 retained by the locator of the applier of FIG. 20.

FIG. 29 is an enlarged, cross-sectional view of the injection port of FIG. 1 disposed in the locator of the applier of FIG. 20 after the applier has been actuated to rotate the applier actuator to the deployed position.

FIG. 30 is a diagrammatic drawing showing an injection port connected to an adjustable gastric band wrapped around an upper part of a stomach.

FIG. 31 depicts a block diagram of components of an exemplary modified version of the injection port of FIG. 1.

Reference will now be made in detail to the present preferred embodiment of the invention, an example of which is illustrated in the accompanying drawings.

DETAILED DESCRIPTION

In the following description, like reference characters designate like or corresponding parts throughout the several views. Also, in the following description, it is to be understood that terms such as front, back, inside, outside, and the like are words of convenience and are not to be construed as limiting terms. Terminology used in this patent is not meant to be limiting insofar as devices described herein, or portions thereof, may be attached or utilized in other orientations. Referring in more detail to the drawings, an embodiment of the invention will now be described.

Referring to FIGS. 1-5, there is shown an implantable medical device, more specifically an injection port, generally indicated at 2, which embodies an attachment mechanism constructed in accordance with the present invention. Although the attachment mechanism is illustrated in the figures as being embodied with injection port 2, the attachment mechanism may be used with any implantable medical device for which it is suited, including by way of example only pace makers, vascular access ports, injection ports (such as used with gastric bands) and gastric pacing devices.

Injection port 2 includes septum retainer 4, septum 6 and port body 8. Injection port 2, with the integrally constructed attachment mechanism, also includes one or more fasteners 10, actuator 12 and a plurality of link members 14.

As seen in FIG. 4, septum 6, which may be made of any biocompatible material such as silicone, is disposed partially within internal cavity 16 of septum retainer 4, adjacent annular flat 18. Septum retainer 4, port body 8, and actuator 12 may be made of any suitable biocompatible material having sufficient stiffness and strength, such as polyetheretherketon (known as PEEK). Fasteners 10 and link members 14 may be made of any suitable biocompatible material, such as stainless steel.

Port body 8 includes annular rim 20, which engages the upper surface of septum 6 about an annular portion. Port body 8 is retained to septum retainer 4 by a plurality of pins 22 which are disposed through respective holes 24 formed in recesses 24 a in port body 8 and which extend inwardly into respective recesses 26 formed about the bottom periphery of septum retainer 4. Pins 22 may be made of any suitable biocompatible material, such as stainless steel.

The uncompressed height of septum 6 is approximately 5 mm around the outer diameter and the uncompressed diameter is approximately 18 mm. The exposed diameter for access to reservoir 20 is approximately 14 mm. The distance between the lower surface of annular rim 20 and annular flat 18 is approximately 4 mm, such that septum 6 is compressed approximately 20% to be adequately self healing to maintain a fluid tight system under pressure and still allow a low profile.

Plate 28 is disposed in recess 16 a formed in the bottom of septum retainer 4, underlying septum 6 and fluid chamber or reservoir 30. As seen in FIG. 4, plate 28 does not contact sidewall 16 b. In the embodiment depicted, plate 28 is metallic, such as stainless steel. When a needle is inserted through septum 6 to introduce or withdraw fluid from fluid chamber 30, such as in order to adjust the size of an adjustable gastric band, metallic plate 28 will protect septum retainer 4 from puncture and provide tactile feedback to the surgeon through the needle indicating that the needle has bottomed in reservoir 30. Plate 28 may be secured to septum retainer 4 in any suitable manner. In the embodiment depicted, plate 28 is held in place by retaining lip 4 a extending over the periphery of plate 28 as best seen in FIGS. 4, 28 and 29. Initially, retaining lip 4 a extends upwardly as an annular lip, providing clearance for insertion of plate 28 into the recess at the bottom of septum retainer 4, and retaining lip 4 a is then rolled or otherwise deformed to overlie at least a portion of the periphery of plate 28 thereby retaining plate 28. In the embodiment depicted the diameter of recess 16 a is smaller than the diameter of sidewall 16 b, providing room to form the annular lip and to deform it into retaining lip 4 a. Plate 28 could be insert molded, with retaining lip 4 a molded as illustrated.

Septum retainer 4 includes passageway 32, in fluid communication with fluid chamber 30, which is defined by fitting 34 extending from the periphery adjacent the bottom of retainer 4. Tube 36, which in the embodiment depicted, leads to an adjustable gastric band (not shown), is connected to fitting 34, being compressingly urged against annular rib 38 by connector 40, which is disposed about tube 36 and secured to port body 8 as described below. Sleeve 42 is disposed about tube 36, secured to connector 40 by annular ribs 44. Sleeve 42 relieves strain on tube 36, preventing tube 36 from kinking when loaded laterally.

Actuator 12 is secured to port body 8. Although in the embodiment depicted actuator 12 is illustrated as an annular ring rotatably supported by port body 8, actuator 12 may be any suitable configuration and supported in any suitable manner to permit actuator 12 to function to move fasteners 10 between and including deployed and undeployed positions. As seen in FIG. 5, port body 8 includes a plurality of downwardly and outwardly extending tabs 46. In the embodiment depicted, there are four equally spaced tabs 46. Actuator 12 includes an equal number of corresponding recesses 48, each having arcuate bottom 50. To assemble actuator 12 to port body 8, recesses 48 are aligned with tabs 46, and pushed down, temporarily deflecting tabs 46 inwardly until tabs 46 reach recesses 48 and move outwardly to dispose lower edges 46 a in recesses 48 such that actuator is retained thereby. The lengths of tabs 46 and depth of recesses 48 allow some axial end play between actuator 12 and port body 8, as will be described below.

Actuator 12 may rotate generally about the central axis of port body 8. In the embodiment depicted, actuator 12 may rotate through an angle of about 40 degrees, although any suitable angle may be used. In the embodiment depicted, when actuator 12 is rotated in the deploying direction, causing fasteners 10 to move to the deployed position, rotation of actuator 12 beyond the fully deployed position is limited by end 48 c contacting tab 46.

A detent system is formed by a pair of spaced apart raised detent ribs 48 a, 48 b extending inwardly from the wall of each recess 48, and a corresponding raised rib 46 b extending outwardly from tab 46. The detent system assists in preventing actuator 12 from rotation and fasteners 10 from moving out of fully retracted or fully extended fired states under vibration or incidental loads, as described below.

Actuator 12 includes a plurality of spaced apart openings or slots 54, which may be engaged by any suitable instrument to transmit the necessary torque to actuator 12 to extend fasteners 10 to the actuated position. Slots 54 are configured to be engaged by commercially available instruments, rectangular in the embodiment depicted, or by the dedicated applier described below. Port body 8 includes a plurality of recesses 56 disposed about its lower periphery which are configured to cooperate with the dedicated applier as described below.

Referring also to FIGS. 6 and 7, septum retainer 4 includes a plurality of locating tabs 58 extending outwardly from adjacent the bottom periphery of septum retainer 4. Locating tab 58 a may be integral with fitting 34. Tabs 58 and 58 a are located in respective complementarily shaped recesses 60 formed in the inner surface of port body 8, aligning septum retainer 4 properly with port body 8.

FIG. 6 illustrates fasteners 10 in the retracted position. As can be seen, fasteners 10 are disposed in respective recesses or slots 60 formed in port body 8. FIG. 7 illustrates fasteners 10 in the extended, or fired, position, extending from slots 60. Rotation of actuator 12 moves fasteners 10 from the retracted position to the extended position.

FIGS. 8-11 are a series of figures illustrating the operation of actuator 12 and one of the plurality of fasteners 10, it being understood that the operation on one of fasteners 10 may be the same as for all fasteners 10, which may, in one embodiment, be moved from a deployed position to an undeployed position simultaneously. FIG. 8 illustrates fastener 10 in a fully retracted state, the undeployed position, disposed completely within slot 62 such that sharp tip 64 is not exposed. This prevents tip 64 from accidentally sticking the surgeon or penetrating any object. Actuator 12 is illustrated rotated counter clockwise as far as permitted by recesses 48 and tabs 46. In this position, ribs 46 b are disposed clockwise of ribs 48 b, as seen in FIG. 14. First ends 14 a of link members 14 are rotatably carried by actuator 12, spaced apart at positions corresponding to the positions of fasteners 10. Second ends 14 b are disposed within openings 66 of fasteners 10.

To actuate the attachment mechanism, integral actuator 12 is rotated in a deploying direction, which in one embodiment as depicted is clockwise (any suitable direction configured to actuate the attachment mechanism may be used), and rib 46 b passes rib 48 b, which may produce an audible signal in addition to a tactile signal to the surgeon. Second end 14 b of link member 14 is free to move within slot 66 during actuation, as the force that rotates fastener 10 into the extended position is transmitted to fastener 10 through the interaction between cam surface 68 of fastener 10 and actuating cam surface 70 of actuator 12. As actuator 12 rotates clockwise, actuating cam surface 70 engages and pushes against cam surface 68, rotating fastener 10 about pivot pin 22. The majority of the force from actuating cam surface 70 acts tangentially on cam surface 68, off center relative to pivot pin 22, causing fastener 10 to rotate. During actuation, end 14 b of link member 14 remains free to move within slot 66, applying no driving force to rotate fastener 10.

In FIG. 9, fastener 10 is rotated about half way though its range of rotation, about 90 degrees as a result of the clockwise rotation of actuator 12. As actuator 12 is rotated clockwise, the force between actuator cam surface 70 and cam surface 68 causes actuator 12 to move upward slightly as allowed by the tolerancing of the components. As actuator 12 is rotated further clockwise from the position shown in FIG. 9, actuator cam surface 70 continues to engage and push against cam surface 68, rotating fastener 10 further counterclockwise.

In FIG. 10, actuator 12 is rotated clockwise to its fullest extent, with rib 46 b having been urged past detent rib 48 a (see FIG. 15). In this position, fastener 10 has rotated to its fullest extent, almost 180 degrees in the embodiment illustrated, with tip 64 disposed within recess 62. In this position, actuator cam surface 70 is over center, and actuator 12 is resistant to being back driven by an undeploying force imparted to fastener 10 as cam surface 68 acts against actuator cam surface 70 in a direction that tends to push actuator 12 up instead of rotating actuator 12. The distal end portion of fastener 10 is configured essentially as a beam, depicted as having a generally rectangular cross section along its length, tapering to sharp tip 64. With fastener 10 extending approximately 180 degrees in the fully extended state, the deployed position, forces which might act on fasteners 10 tend to act through the pivot axis defined by pivot pin 22, instead of rotating fasteners 10. It is noted that although pin 22 is illustrated as being a separate piece from fastener 10, the two may be integral or even of unitary construction.

If it is desirable to retract fasteners 10, such as to remove or reposition the implanted device, actuator 12 may be rotated in an undeploying direction, counterclockwise in one embodiment depicted. Starting with the position of actuator 12 shown in FIG. 10, actuator 12 may be rotated counterclockwise, with actuator cam surface 70 sliding against cam surface 68, without rotating fastener 10. In the embodiment depicted, continued counterclockwise rotation of actuator 12 moves cam surface 70 out of contact with cam surface 68, with no substantial rotating force being exerted on fastener 10 until second end 14 b of link member reaches a location in slot 66, such as at one end of slot 66, at which link member 14 begins pulling against slot 66 causing fastener 10 to rotate and begin to retract.

As seen in FIG. 11, actuator 12 has been advanced counterclockwise compared to the position shown in FIG. 10, and fastener 10 is rotated approximately halfway through its range. As can be seen by comparing FIG. 9 to FIG. 11, actuator 12 is in different positions with fastener 10 in the same position, in dependence upon whether the attachment mechanism is being actuated or deactuated (retracted). This results from the lost motion that results when link member 14 is pulling on slot 66 in comparison to actuator cam surface 70 pushing directly on cam surface 68. To retract fasteners 10 fully, actuator 12 is rotated until detent rib 46 b snaps past detent rib 48 b.

Referring to FIG. 8, when fasteners 10 reach the fully undeployed position tip 64 may be disposed fully in slot or recess 62. Further undeploying rotation of actuator 12 is prevented by link member 14 which is prevented from further movement by fastener 10.

Referring to FIGS. 2 and 3, actuator 12 includes openings 52 a formed therethrough, which align with corresponding openings 52 b formed in port body 8 when actuator is in the undeployed position. Openings 52 a and 52 b may be used by the surgeon to suture injection port 2 if the integral attachment mechanism is not used.

Referring to FIGS. 12 and 13, the attachment mechanism is shown without actuator 12. Link members 14 are shown in their actual positions when first ends 14 a are supported by actuator 12, in the deployed and in the undeployed states.

Referring to FIGS. 14 and 15, there is illustrated a top view of the visual position indicator and a portion of the actuator ring detent system of the attachment mechanism as embodied in injection port 2. In FIG. 14, the attachment mechanism is in the retracted, undeployed state or position. In this position, detent rib 46 b is clockwise of detent rib 48 b, and thus in the undeployed detent position. In FIG. 15, the attachment mechanism is in the actuated or deployed position. In this position, detent rib 46 b is counterclockwise of detent rib 48 b, and thus in the deployed detent position.

FIGS. 14 and 15 illustrate a visual indicator of the state of the attachment mechanism. As seen in FIG. 14, indicia may be utilized, such as an unlocked lock icon 72 and a locked lock icon 74 molded integral with actuator ring 12. Any suitable graphic indicator may be used, and may be printed on or otherwise applied in a suitable manner. Port body 8 may include indicator 76 to provide a reference point for the movable indicia. Arrow 78 may be included to indicate the bidirectional motion of actuator 12.

FIGS. 16-18 illustrate the locking connection between connector 40 and port body 8. FIG. 16 is an exploded perspective view showing fitting 34 partially surrounded by extension 78. FIG. 17 shows extension 78 in cross-section, with connector 40 generally disposed about fitting 34 and tube 36 aligned in circumferential slot 78 c of extension 78. Connector 40 includes a pair of tabs 40 a, 40 b, extending outwardly therefrom. To assemble, connector 40 is guided along tube 36 and fitting 34, with tabs 40 a and 40 b aligned with openings 78 a and 78 b of extension 78. With tabs 40 a and 40 b aligned with circumferential slot 78 c, connector 40 is rotated to lock it in place. During rotation, detent edge 78 d creates interference opposing the rotation of tab 40 a, but is dimensioned to allow tab 40 a to be rotated past, to the locked position seen in FIG. 18.

FIG. 19 illustrates safety cap 80 which may be removably secured to the bottom of injection port 2 to cover fasteners 10 to protect users from accidental exposure to sharp tips 64 while handling injection port 2. Safety cap 80 includes body 82 with annular rim 84 and raised center 86 defining annular recess 88. Safety cap 80 may be oriented and retained to injection port through any suitable configuration. As depicted, body 82 includes a plurality of arcuate retention tabs 90 extending upwardly from raised center 86. Arcuate retention tabs 90 are shaped complementarily to corresponding arcuate slots 92, best seen in FIGS. 3, 6 and 7, and may have ribs as shown. Safety cap 80 is secured to injection port 2 by inserting arcuate retention tabs 90 into arcuate slots 92, which are sized to retain tabs 90. Fasteners 10 are thus aligned with annular recess 88, which is sized to allow fasteners 10 to be extended without contacting safety cap 80. As depicted, since arcuate retention tabs 90 and arcuate slots 92 are respectively the same size and equally spaced, safety cap 80 is not indexed to a particular position, and may be secured to injection port 2 in four different positions. Safety cap 80 includes pull tab 94 with raised a plurality of ribs 96 to provide a better gripping surface. Although pull tab 94 may be oriented in any suitable orientation, in the embodiment, the relative position between pull tab 94 and arcuate retention tabs 90 locates pull tab at 45 degrees to the direction of connector 40. Tabs 90 and slots 92 may be of any suitable shape.

As mentioned previously, the attachment mechanism may be actuated by engaging slots 54 with commercially available instruments or by a dedicated applier. FIG. 20 illustrates applier, generally indicated at 100, which is configured to position, actuate, deactuate, remove or reposition injection port 2. It is noted that the practice of aspects of the present invention as applied to an applier is not limited to the specific applier embodiment depicted herein.

As shown in FIG. 20, applier 100 includes body 102, locator 104, actuator 106 and safety switch 108. As will be described below, injection port 2 may be assembled to locator 104, with extension 78 and tab 96 disposed in alignment slots 110 and 112. Locator 104 is angled relative to body 102, allowing for easier and better visualization of injection port 2 during implantation. In the embodiment depicted, the angle is 20 degrees and the shaft portion of body 102 is 10 cm.

Referring to FIG. 21, body 102 includes first and second halves 102 a and 102 b assembled to each other to contain the internal components. Except for locating pins 202, pivot pins 114 and ship laps, body halves 102 a and 102 b are substantially similar to each other. Locating pins 202, illustrated as extending from body half 102 a, fit into respective complementarily shaped openings (not illustrated) on body half 102 b. The engagement of the plurality of locating pins 202 in the openings is sufficient to hold body halves 102 a and 102 b together. Pins 202 may alternatively extend from body half 102 b with the openings carried by body half 102 a. Any suitable configuration may be used to assemble and secure body halves 102 a and 102 b together.

Actuator 106 includes first and second halves 106 a and 106 b. Locating pins 204, illustrated as extending from actuator half 106 a, fit into respective complementarily shaped openings (not illustrated) on actuator half 106 b. Pins 204 may alternatively extend from actuator half 106 b with the openings carried by actuator half 106 a. Any suitable configuration may be used to assemble and secure actuator halves 106 a and 106 b together. Body half 102 b includes pivot pin 114 b which rotatably supports actuator 106 at one end, extending through pivot holes 116 a and 116 b into opening 114 a. Body half 102 a includes pivot pin 118 b (see FIG. 22) which rotatably supports safety switch 108. Body halves 102 a and 102 b, locator 104, actuator halves 106 a and 106 b, and safety switch 108 may be made of any biocompatible material such as polycarbonate.

Referring to FIGS. 21-24, applier 100 includes cam 120, drive shaft 122 with flexible shaft 124, drive shaft pin 126, cam return spring 128, safety biasing spring 130, and actuator 132. Actuator 132 is configured to effect the deployment or undeployment of the attachment mechanism of the medical implant. Cam 120 includes shaft 134 and cam collar 136. The upper end of shaft 134 has a “T” configuration terminating in cross member 138. Cam collar 136 defines a hollow interior and a pair of spaced apart, complementarily shaped cam tracks 140 a and 140 b formed on opposite sides of cam collar 136. Upper end 122 a of drive shaft 122 is disposed partially within the hollow interior defined by cam collar 136, captured therein by drive shaft pin 126. Drive shaft pin 126 is sized such that each end is located within a respective cam track 140 a, 140 b. The length of the hollow interior allows upper end 122 a to reciprocate therein, with cam tracks 140 a and 140 b imparting rotation to drive shaft 122 through drive shaft pin 126 during reciprocation. Cam 120, drive shaft 122 and actuator 132 may be made of any suitable material having sufficient stiffness and strength. In the embodiment depicted, cam 120 and actuator 132 are made of a liquid crystal polymer such as Vectra™ LCP, and drive shaft 122 is made of a PPE+PS such as Noryl™. Drive shaft pin 126 and cam return spring 128 may be made of any suitable material, such as stainless steel.

Cam 120 is retained between body portions 102 a and 102 b, and in one embodiment, such as that depicted can reciprocate. Cam collar 136 has spaced apart, generally flat outer surfaces 142 a and 142 b tracks through which 140 a and 140 b are formed. These surfaces 140 a and 140 b are disposed between guide walls 144 a and 144 b formed in body portions 102 a and 102 b. Cam collar 136 also includes oppositely facing channels 146 a and 146 b (see FIG. 23), which are guided for axial reciprocation by guides 148 a and 148 b (not illustrated) formed in body portions 102 a and 102 b, respectively. The upper end of shaft 134 and cross member 138 are disposed sandwiched between actuator halves 106 a and 106 b. Each actuator half 106 a, 106 b, includes a cam track 150 defined by a pair of spaced apart walls 150 a and 150 b extending from the interior surfaces of actuator halves 106 a and 106 b. Cam track 150 is configured to receive and guide cross member 138 as actuator 106 is rotated about pin 114, forcing cam 120 to advance linearly downwardly into body 102.

Drive shaft 122 includes annular collar 152 which is received in slots 154 a and 154 b (not illustrated) formed in body halves 102 a and 102 b, respectively. Slots 154 a and 154 b rotatably support drive shaft 122. Drive shaft 122 and cam 120 are generally aligned and collinear with each other, defining the axis of the shaft portion of body 102. As cam 120 is advanced downwardly, drive shaft pin 126 follows cam tracks 140 a and 140 b, causing drive shaft 122 to rotate, thus converting linear motion to rotary motion. Cam return spring 128 provides a nominal return force against cam collar 136.

Flexible shaft 124 is supported by a plurality of ribs 156, formed in each body half 102 a, 102 b, which support the bend in flexible shaft 124 that permits the rotary motion to be transferred to actuator 132 which is disposed at an angle relative to the shaft of body 102. Flexible shaft 124 may be made of any suitable biocompatible material, such as stainless steel. In an embodiment depicted, flexible shaft 124 has a stranded construction, with a center core having multiple layers of wire wrapped thereabout. Ends 124 a and 124 b of flexible shaft 124 may be attached to end 122 b and actuator 132, respectively, in any suitable manner which sufficiently limits rotational end play to prevent or minimize lost rotational motion. In an embodiment depicted, end 124 a was overmolded into end 122 b, and end 124 b was press fit into actuator 132. Alternatively, end 124 a could be press fit into end 122 b, and end 124 b overmolded into actuator 132, both could be press fit, or both could be overmolded (with a corresponding change to the configuration of locator 104 to allow assembly.

Referring to FIGS. 21-25, actuator 132 includes disc shaped member 158 and shaft 160 extending upwardly therefrom. The upper end of shaft 160 includes a pair of outwardly extending tabs 162 a and 162 b. Locator 104 includes hub 164 defining bore 166 therethrough. Bore 166 is shaped to receive and rotatably support shaft 160, and includes two outwardly extending arcuate recesses 168 a and 168 b configured to provide assembly clearance for tabs 162 a and 162 b, allowing hub 164 to be inserted into bore 166. The lengths of shaft 160 and hub 164 are sized such that tabs 162 a and 162 b are located above upper surface 164 a of hub 164, allowing rotation of actuator 132 while retaining it axially relative to hub 164. Stops 170 and 170 b extend upwardly from upper surface 164 a, limiting the rotation of actuator 132. Bore 166 defines a central axis of locator 104 about which actuator 132 is rotated. The central axis of locator 104 is disposed at an angle to the axis of the shaft portion of body 102, as previously mentioned.

Hub 164 includes a pair of oppositely extending tabs 172 a and 172 b which retain port actuator 104 to body 102 and prevent rotation. Body halves 102 a and 102 b include respective recesses 174 a (see FIG. 21) and 174 b (not illustrated) shaped complementarily to tabs 172 a and 172 b.

Referring also to FIGS. 26 and 27, disc shaped member 158 of actuator 132 is seen disposed within locator 104. Actuator 132 includes a pair of spaced apart posts 176 a and 176 b, extending from adjacent periphery 158 a of member 158. Posts 176 a and 176 b are shaped complementarily with openings 54. In the embodiment depicted, the distal ends of posts 176 a and 167 b are tapered to assist in guiding posts 176 a and 176 b into openings 54. Any suitable configuration may be utilized to create releasable contact between actuator 132 and actuator 12 capable of actuating actuator 12.

Disc shaped member 158 also includes a pair of spaced apart cams 178 a and 178 b which extend outwardly and upwardly from periphery 158 a of member 158. FIG. 27 illustrates cam 178 a at a cross-section taken near the bottom surface of member 158. Cams 178 a and 178 b include ramps 180 a and 180 b which start at periphery 158 a and lead out to surfaces 182 a and 182 b, respectively. Each surface 182 a, 182 b is arcuate, shown in the embodiment depicted as generally having a constant radius.

In the embodiment depicted, locator 104 includes a pair of spaced apart cantilever arms 184 a and 184 b, each having rib 186 a and 186 b, respectively. For clarity, FIG. 27 illustrates arm 184 a in cross-section taken through rib 186 a, at the same level as for cam 178 a. At their distal ends, arms 184 a and 184 b include respective inwardly extending flanges 188 a and 188 b. Flanges 188 a and 188 b are shaped complementarily to recesses 56 on port body 8, configured to engage ledges 56 a when injection port 2 is retained by locator 104.

In the embodiment depicted, in the non-actuated state, posts 176 a and 176 b are generally aligned with arms 184 a and 184 b, respectively, although posts 176 a and 176 b may be at any position that corresponds to position of the actuating feature of actuator 12, which in the embodiment depicted is openings 54. As actuator 106 is depressed, actuator 132 rotates (counterclockwise in the embodiment depicted when viewed from the bottom), advancing cams 178 a and 178 b such that ramps 180 a and 180 b contact ribs 186 a and 186 b, respectively, deflecting arms 184 a and 184 b outwardly. When surfaces 182 a and 182 b engage ribs 186 a and 186 b, arms 184 a and 184 b are deflected a distance sufficient to move flanges 188 a and 188 b to a position where they no longer extend into recesses 56 or contact ledges 56 a, thus releasing injection port 2 from locator 104.

FIG. 28 illustrates injection port 2 disposed in and retained by locator 104, with extension housing 78 and tab 96 disposed in slots 110 and 112, respectively (see FIG. 20, not seen in FIG. 28). As depicted, posts 176 a and 176 b extend into openings 54 of actuator 12, and flanges 188 a and 188 b extending into recesses 56 proximal ledges 56 a. Safety cap 80 is connected to injection port 12 when injection port 12 is inserted into locator 104, covering fasteners 10 (not seen in FIG. 28).

Referring also to FIGS. 20 and 22, to insert injection port 2 into locator 104, actuator 106 is oriented in the undeployed position so that actuator 132 is in the undeployed position. Actuator 12 is oriented in the undeployed position, and inserted into locator 104, with extension housing 78 and tab 96 disposed in slots 110 and 112, respectively.

Actuator 106 may, as illustrated in FIG. 20, include a visual indicator to indicate whether actuator 106 is fully in the undeployed state, such as unlocked lock icon 190, and indicia to indicate whether actuator 106 is in the deployed state, such as locked lock icon 192. Such visual indication may be include by any suitable manner, such as by molding integral with actuator 106, applying as a adhesive film or such, or printing directly on actuator 106. With the indicator illustrated, unlocked lock icon 190 is visible adjacent the upper edge of body 102, although other configurations of indication may be utilized, such as a window or such formed in body 102 to reveal the indicia.

To use, locator 104 and a portion of 102, if necessary, is inserted through an incision by the surgeon and located in the desired position adjacent the body tissue to which the medical implant (which in the embodiment depicted is an injection port 2) is to be attached. The angle between locator 104 and body 102 allows the surgeon to visualize the site directly. With injection port 2 in position, the one or more fasteners 10 are moved from the undeployed position to the deployed position in an annular path to engage the tissue. Fasteners 10 allow injection port 2 to be secured to the tissue with a retention strength equal to or greater than when secured with sutures. Safety switch 108 is rotated about pivot pin 118, withdrawing lockout tab 194 from lower opening 196, allowing actuator 106 to be rotated about pivot pin 114. This action causes cam track 150 to move cross member 138 downward, causing cam collar 136 to rotate drive shaft 122, thereby rotating actuator 132 relative to locator 104.

Rotation of actuator 132 actuates actuator 12 by rotating it. The engagement between extension 78 and tab 96 and slots 110 and 112, respectively, prevent port body 8 from rotating, allowing relative motion between actuator 12 and port body 8.

Once actuator 106 reaches the deployed position, lockout tab 194 is urged into upper opening 198, retaining actuator 106 in the deployed position. In the embodiment depicted, spring 130 biases lockout tab 194 sufficiently to produce sound as lockout tab 194 snaps into upper opening 198, providing an audible signal that actuator 106, and therefore actuator 12 and fasteners 10 are deployed fully. As illustrated in FIG. 29, with actuator 106 in the deployed position, actuator 12 has been rotated and fasteners 10 are in the deployed position having penetrated the body tissue, such as the rectus sheath. Cams 178 a and 178 b have been rotated to a position where surfaces 182 a and 182 b are adjacent ribs 186 a and 186 b, with arms 184 a and 184 b deflected outwardly such that flanges 188 a and 188 b are not disposed in recesses 56 and not engaging ledges 56 a. With injection port 2 secured to the body tissue, and released from locator 104, the surgeon may withdraw locator 104, leaving injection port 2 in place. If a visual indicator of the state of the attachment mechanism is included with the implant, the surgeon can tell whether the attachment mechanism is fully deployed.

The attachment mechanism embodied in injection port 2 is configured to be reversible so that the medical implant, injection port 2, may be moved, such as to reposition it or remove it from the patient. To do so, with actuator 106 in the deployed position, locator 104 is placed over injection port 2, locating extension 78 and tab 96 in slots 110 and 112 so that posts 176 a and 176 b are engaged with recesses 54. Safety switch 108 is rotated to withdraw lockout tab 194 from upper opening 198, while the surgeon pulls up on extension 200 of actuator 106. Although cam return spring 128 urges cam collar 136 upwardly, extension 200 allows an additional return force to be applied. As cross member 138 is pulled up by cam track 150, actuator 132 rotates actuator 12, moving fasteners 10 from the deployed position to the undeployed position simultaneously, while cams 178 a and 178 b disengage from ribs 186 a and 186 b, allowing flanges 188 a and 188 b to engage recess 56 and ledge 56 a so as to retain injection port 2 in locator 104. When actuator 106 has been moved to the undeployed position, lockout tab 194 snaps into lower opening 196, generating an audible signal that actuator 106 is undeployed fully, and injection port 2 is detached from the body tissue and may be relocated or removed.

In FIG. 30, adjustable gastric band 210 is shown wrapped around an upper portion of stomach 212, kept in place by attaching the two ends together and extending portion 214 of the stomach 212 over adjustable gastric band 210 by suturing portion 214 to the stomach. One end of flexible conduit 216 is in fluid communication with the internal cavity of the balloon (not shown), with the other end being in fluid communication with an internal cavity of injection port 218. At the time adjustable gastric band 210 is implanted around a portion of the stomach, remote injection port 218 is also implanted at a suitable location, usually within the rectus sheaths, for transcutaneous access via a Huber needle.

FIG. 31 depicts a schematic diagram of an exemplary alternative port 1100 that is operable to provide haptic feedback in response to palpation and/or other types of stimulus as will be described in greater detail below. Port 1100 of this example includes a feedback interface ring 1202, a processor 1204, an interface sensor 1206, a power source 1208, a vibration generator 1210, a storage device 1212, a telemetry transceiver coil 1214, and a pressure sensor 1216. Port 1100 of this example is otherwise configured identically to port 2 described above.

In the present example, haptic feedback interface ring 1202 is positioned between actuator 12 and port body 8. Haptic feedback interface ring 1202 is operable to sense when actuator 12 is being pushed downwardly toward port body 8. Furthermore, and as will be described in greater detail below, port 1100 may provide a vibratory response when interface ring 1202 senses that actuator 12 is being pushed downwardly toward port body 8. This vibratory response may assist a physician in locating port 1100 through external palpation after port 1100 has been implanted in a patient. Interface ring 1202 may comprise or form a switch that is in communication with a processor 1204 (e.g., via wire, etc.) as will be described in greater detail below. Actuation of interface ring 1202 by pushing downward on actuator 12 (e.g., by a physician palpating a patient, etc.) may thus actuate the corresponding switch, which may cause processor 1204 to trigger the vibratory response.

In some versions, port 1100 comprises one or more resilient members (not shown) that are configured to bias actuator 12 to an upper position. By way of example only, interface ring 1202 may itself be configured to bias actuator 12 to an upper position. For instance, interface ring 1202 may be resilient and may have a “wavy” configuration. Other ways in which actuator 12 may be biased to an upper position (regardless of whether actuator 12 is also rotatable) will be apparent to those of ordinary skill in the art in view of the teachings herein. Similarly, other suitable variations, components, features, and configurations of interface ring 1202 will be apparent to those of ordinary skill in the art in view of the teachings herein. By way of example only, interface ring 1202 may be substituted with one or more switches positioned between actuator 12 and port body 8, without a ring-shaped member being used to form a vibratory response activation interface between actuator 12 and port body 8. Such discrete switches may be equidistantly positioned about a circumference or be positioned in any other suitable locations/arrangement. As another merely illustrative example, port 1100 may be configured such that interface ring 1202 does not move up and down relative to port body 8. In some such versions, one or more strain gauges or other types of sensors may be used to determine whether a downward force is being exerted on actuator 12, with such sensors being configured to trigger a vibratory response as described in greater detail below. Alternatively, interface ring 1202 may be omitted in some versions, including but not limited to those versions described in greater detail below.

In addition to providing some degree of axial play of actuator 12, port 1100 may provide some degree of axial play for plate 28. In other words, plate 28 may slightly move up or down along the same axis about which actuator 12 rotates. Such axial play may be provided without sacrificing a hermetic seal between plate 28 and septum retainer 4 or between plate 28 and port body 8. In some versions, haptic feedback interface sensor 1206 is positioned beneath plate 28. Interface sensor 1206 is operable to sense when plate 28 is being pushed downwardly. Furthermore, and as will be described in greater detail below, port 1100 may provide a vibratory response when interface sensor 1206 senses that plate 28 is being pushed downwardly. This vibratory response may assist a physician in determining that a needle has struck plate 28, which may further indicate that the needle has been successfully inserted through septum 6. Interface sensor 1206 may comprise or form a switch that is in communication with processor 1204 (e.g., via wire, etc.) as will be described in greater detail below. Actuation of interface sensor 1206 by pushing downward on plate 28 (e.g., by a needle striking plate 28, etc.) may thus actuate the corresponding switch, which may cause processor 1204 to trigger the vibratory response.

In some versions, port 1100 comprises one or more resilient members (not shown) that are configured to bias plate 28 to an upper position. By way of example only, interface sensor 1206 may itself be configured to bias actuator 12 to an upper position. For instance, interface sensor 1206 may comprise a resilient ring positioned between the outer perimeter of the underside of plate 28 and septum retainer 4, and such a ring may have a “wavy” configuration. Other ways in which plate 28 may be biased to an upper position will be apparent to those of ordinary skill in the art in view of the teachings herein. Similarly, other suitable variations, components, features, and configurations of interface sensor 1206 will be apparent to those of ordinary skill in the art in view of the teachings herein.

In some other versions, port 1100 may be configured such that plate 28 does not move up and down relative to septum retainer 4 and/or port body 8. It should be understood that, in some such versions, various types of interface sensors 1206 may still be used to determine whether a downward force is being exerted on plate 28, with such sensors being configured to trigger a vibratory response as described in greater detail below. For instance, interface sensor 1206 may comprise a thin film capacitive switch or strain gauge on plate 28. As yet another merely illustrative example, interface sensor 1206 may simply detect the presence of a needle in fluid chamber 30, without necessarily detecting contact between the needle and plate 28 as such. For instance, interface sensor 1206 may comprise a proximity sensor, an ultra wideband radar device, a metal detector that essentially ignores the metal of plate 28 while detecting the metal of a needle in fluid chamber 30, etc. Furthermore, it should be understood that interface sensor 1206 need not necessarily be located under plate 28 (e.g., interface sensor 1206 may be in fluid chamber 30, etc.). Still other suitable components and configurations that may be used for interface sensor 1206 will be apparent to those of ordinary skill in the art in view of the teachings herein. Alternatively, interface sensor 1206 may be omitted in some versions, including but not limited to those versions described in greater detail below.

Injection port 1100 may also include a chamber (not shown) located below plate 28. The chamber may be enclosed and hermetically sealed, such that it is fluidly isolated relative to fluid chamber 30. This extra chamber may enclose several electrical components that are configured to provide vibratory responses as noted above. For instance, the extra chamber may enclose processor 1204, interface sensor 1206, a power source 1208, a vibration generator 1210, and a storage device 1212 (e.g., flash memory, memory chip, etc.). Of course, any or all of these components may be located elsewhere if desired. While these components are only shown in block form in the drawings, the various structural forms that these components may take will be apparent to those of ordinary skill in the art in view of the teachings herein. Interface ring 1202, interface sensor 1206, power source 1208, vibration generator 1210, and storage device 1212 are all in communication with processor 1204 (e.g., via wires and/or traces in a circuit board, etc.). Processor 1204 may comprise an off the shelf microprocessor, a customized processor 1204, or any other suitable type of device or component. Processor 1204 is configured to receive input from interface ring 1202 and interface sensor 1206, and is configured to trigger vibratory responses through vibration generator 1210 as will be described in greater detail below. Processor 1204 is also configured to interrogate storage device 1212, and may also be configured to cause data to be stored on storage device 1212.

Power source 1208 of the present example comprises a conventional battery. It should be understood, however, that power source 1208 may instead be substituted with a transcutaneous energy transfer (TET) coil, such that components shown in FIG. 31 are powered remotely by a coil that is external to the patient. For instance, in versions where port 1100 includes a telemetry transceiver coil 1214 as described in greater detail below, such a transceiver coil 1214 may serve a dual role of receiving TET power and providing telemetric communication of data. As another merely illustrative example, where power source 1208 comprises a battery, such a battery may be recharged through TET power. Still other suitable ways in which power may be provided to electrical/electronic components of port 1100 will be apparent to those of ordinary skill in the art in view of the teachings herein.

In some versions, interface ring 1202 and/or interface sensor 1206 are omitted. In some such versions, vibration generator 1210 is activated by an external coil. For instance, such an external coil may be configured in accordance with the teachings of U.S. Pub. No. 2006/0211914, entitled “System and Method for Determining Implanted Device Positioning and Obtaining Pressure Data,” published Sep. 21, 2006, the disclosure of which is incorporated by reference herein. Other suitable forms that such an external coil may take will be apparent to those of ordinary skill in the art in view of the teachings herein. In some versions where vibration generator 1210 is activated by an external coil, telemetry transceiver coil 1214 may be communicatively and transcutaneously coupled with the external coil. In particular, transceiver coil 1214 and processor 1204 may respond to a field generated by the external coil by activating vibration generator 1210. In addition, the external coil and telemetry transceiver coil 1214 may together provide power to vibration generator 1210 via TET. Thus, a battery or other implanted power source 1208 need not be included within port 1100. It should be understood from the foregoing that a physician may locate port 1100 by sweeping over the patient's abdomen and/or chest with the external coil until vibrations are felt from vibration generator 1210. Such vibrations may reach a maximum intensity when the external coil is directly over port 1100. The physician may then insert the needle through the center of external coil to reach port 1100; or may first remove external coil then insert the needle where the center of the external coil was when vibrations from vibration generator 1210 were at their maximum intensity.

In some versions where an external coil is used to activate vibration generator 1210, vibration generator 1210 comprises a conventional type of vibration generator (e.g., such as those described in greater detail below, etc.). In some such versions, the external coil simply activates vibration generator 1210, which is actually powered by power source 1208 within port 1100. In other words, the field generated by the external coil simply acts as a switch to cause vibration generator 1210 to generate vibrations. In some other versions where vibration generator 1210 comprises a conventional type of vibration generator, the external coil provides power to vibration generator 1210 through TET as described above. Of course, vibration generators 1210 that are turned on by an external coil and/or are powered by an external coil need not be conventional, and may take any suitable form. Various forms that vibration generator 1210 may take, as well as various ways in which vibration generator 1210 may operate and be used, are disclosed in U.S. patent application Ser. No. 12/640,048, filed Dec. 17, 2009, entitled “Implantable Port with Vibratory Feedback,” the disclosure of which is incorporated by reference herein.

It should also be understood that vibration generator 1210 may be used for a variety of purposes. One merely exemplary use for vibration generator 1210 may be to assist a physician in locating port 1100 after port 1100 has been implanted in a patient. For instance, depending on the location of port 1100 within the patient and the obesity of the patient, some physicians may have difficulty in locating a conventional implanted port 1100. The physician may wish to locate port 1100 in order to insert a needle into septum 6 to add fluid to or withdraw fluid from the gastric band system. In some settings where port 1100 includes a TET/telemetry coil, the physician may wish to locate port 1100 in order to properly position an external coil or other type of antenna in order to provide power to and/or receive data from components in the port 1100. Accordingly, where port 1100 has been implanted in the patient, the physician may palpate the patient's abdomen and/or chest in order to locate port 1100. When the physician palpates over the location of port 1100, such palpation may press actuator 12 downward, which may activate interface ring 1202, which may in turn activate vibration generator 1210 to provide haptic feedback to the physician indicating that the port 1100 is generally beneath the physician's hand. The physician may then insert the needle in this area to pierce septum 6 in order to add fluid to or withdraw fluid from the gastric band system.

In some settings, actuator 12 may occasionally be pressed down by the patient's own movements or positioning. It may be desirable to prevent such incidental pressing of actuator 12 from triggering a vibratory response by vibration generator 1210. To that end, processor 1204 may be configured to compare downward forces exerted on actuator 12 against a predetermined force threshold level, such that processor 1204 only triggers vibration by vibration generator 1210 when the downward force on actuator 12 exceeds the predetermined threshold. The force threshold may be selected such that incidental pressing on actuator 12 by patient movement/positioning falls below the threshold; while sufficient external palpation by a physician exceeds the threshold. Data representing such a force threshold may be stored on storage device 1212. In some other variations, processor 1204 may be configured such that it will not trigger vibration by vibration generator 1210 unless the presence of some external signal is detected. For instance, control logic in processor 1204 may be configured to cause processor 1204 to ignore activations of interface ring 1202 unless coil 1214 is receiving some type of signal from a coil that is external to the patient. Such an external signal may thus simply “unlock” vibration generator 1210, such that external palpation by a physician may activate vibration generator 1210 only when vibration generator 1210 is “unlocked” by the external signal. Alternatively, an external signal may directly cause vibration generator 1210 to generate vibrations as noted above. Still other suitable ways in which port 1100 may prevent a vibratory response to inadvertent pressing of actuator 12 will be apparent to those of ordinary skill in the art in view of the teachings herein. Of course, some versions of port 1100 may lack such prevention; and some other versions of port 1100 may lack a feature permitting actuator 12 to be pressed in relative to other portions of port 1100.

Another merely exemplary use for vibration generator 1210 may be to assist a physician in confirming that the needle has successfully reached fluid chamber 30 to adjust the amount/pressure of fluid in an implanted gastric band system. For instance, even when a physician has determined the general location of port 1100 implanted in a patient, the physician may have difficulty determining whether a needle inserted in the patient has successfully reached fluid chamber 30. A physician may generally determine through tactile feedback felt through the needle and syringe that the needle has struck some hard object, but the physician may not be able to determine whether the needle has struck plate 28 or some other hard component of port 1100 (e.g., needle may have instead struck actuator 12, port housing 8, etc.). Accordingly, when the physician has successfully inserted the needle into fluid chamber 30 and the needle has struck plate 28, such striking of plate 28 by the needle may activate interface sensor 1206, which may in turn activate vibration generator 1210 to provide haptic feedback to the physician indicating that the needle has reached fluid chamber 30. The physician may then use the syringe and needle to add fluid to or withdraw fluid from the implanted gastric band system, to adjust the size of the stoma created by gastric band 210.

In situations where the physician feels the inserted needle striking something hard but does not receive the vibratory response from vibration generator 1210, such a lack of vibratory response may indicate to the physician that the needle has missed septum 6 (e.g., needle instead struck actuator 12, port housing 8, etc.) and that the needle is therefore not in fluid chamber 30. The physician may then partially or fully withdraw the needle and reposition it for another attempt to pierce septum 6 and reach fluid chamber 30. This process may be repeated until the physician finally receives haptic feedback from vibration generator 1210 to indicate that the needle has successfully reached fluid chamber 30.

In some versions where port 1100 includes both interface ring 1202 and interface sensor 1206, it may be desirable to vary the response from vibration generator 1210 based on whether interface ring 1202 or interface sensor 1206 has been activated. This may be desirable in some settings to account for the possibility that a physician may strike actuator 12 with an inserted needle instead of striking plate 28. Making the vibratory response when interface sensor 1206 is triggered different from the vibratory response when interface ring 1202 is triggered may thus allow the physician to confirm that the inserted needle has struck plate 28 instead of actuator 12. The vibratory response from vibration generator 1210 may differ in a variety of ways, including but not limited to frequency, waveform, magnitude, duration, and/or pulse pattern, etc., based on whether interface ring 1202 or interface sensor 1206 has been activated. Of course, some versions may provide the same vibratory response from vibration generator 1210 regardless of whether interface ring 1202 or interface sensor 1206 has been activated. Furthermore, some versions of port 1100 may have only interface ring 1202 or only interface sensor 1206; while lacking the other.

In some alternative versions, port 1100 lacks interface sensor 1206. In some such versions, vibration generator 1210 is operable to generate externally palpable vibrations based on actuation of interface ring 1202, based on the presence of an externally applied field, or based on some other form of activation. Furthermore, such vibrations may be sustained as a physician inserts a needle into a patient. Alternatively, such vibrations may be initiated upon the needle contacting an external portion of port 1100. In some such versions, vibration generator 1210 may cause the entire port 1100 to vibrate. It should be understood that such vibrations may be acoustically coupled with the needle in different ways depending on the material of the port 1100 that is struck by the needle. For instance, port body 8 (including annular rim 20) and actuator 12 may be formed of a substantially hard material (e.g., plastic and/or metal, etc.); while septum 6 may be formed of a relatively soft material (e.g., silicone, etc.). Thus, when the needle strikes a relatively hard portion of vibrating port 1100, the acoustic coupling may provide a “scratchy” vibratory sensation through the needle to the physician's hand. Such a tactile sensation may inform the physician that the needle is in contact with port 1100 but not inserted through septum 6. The physician may then reposition the needle until the physician feels a “softer” vibratory sensation through the needle that would be associated with the needle being inserted through septum 6 of vibrating port 1100. As one merely illustrative variation of this example, port 1100 may be configured such that vibration is maximized at annular rim 20 surrounding septum 6, which may provide greater guidance to the physician who is attempting to locate septum 6 based on haptic/tactile feedback. For instance, portions of port 1100 that are external to annular rim 20 may be vibrationally isolated or dampened relative to annular rim 20, such that those external portions either do not vibrate while annular rim 20 vibrate or such that the vibrations of those external portions have a lower amplitude than the vibrations of annular rim 20.

Yet another merely exemplary use for vibration generator 1210 may be to provide an alert when some condition has been detected. By way of example only, some versions of port 1100 may include a pressure sensor 1216 that is configured to sense the pressure of fluid in a gastric band system. Various suitable ways in which a pressure sensor 1216 may be incorporated into a gastric band system are disclosed in U.S. Pub. No. 2006/0211914, entitled “System and Method for Determining Implanted Device Positioning and Obtaining Pressure Data,” published Sep. 21, 2006, the disclosure of which is incorporated by reference herein. Alternatively, any other suitable type of pressure sensor 1216 may be incorporated into the gastric band system in any suitable fashion. While FIG. 31 depicts pressure sensor 1216 as a component of port 1100, it should be understood that pressure sensor 1216 may be located in any other suitable position or component.

Processor 1204 may be configured to monitor readings from pressure sensor 1216 and compare those readings to one or more baselines stored on storage device 1212. Processor 1204 may further be configured to trigger a vibratory response by vibration generator 1210 when a pressure data reading from pressure sensor 1216 deviates from a baseline or range. For instance, processor 1204 may trigger a vibratory response by vibration generator 1210 when the pressure of fluid in the gastric band system falls below a threshold (e.g., approximately 10 mmHg, etc.), which may indicate that there is a leak in the system, that more fluid needs to be added to the system, or some other condition. Similarly, processor 1204 may trigger a vibratory response by vibration generator 1210 when the pressure of fluid in the gastric band system exceeds a threshold (e.g., approximately 50 mmHg, etc.), which may indicate that fluid needs to be withdrawn from the system, or some other condition. Such pressure-based feedback may be felt by the patient, and may prompt the patient to contact their physician for an adjustment of gastric band 210. The physician may then investigate further and provide any appropriate medical response (e.g., adding fluid to or withdrawing fluid from the gastric band system, etc.). By way of example only, pressure-based feedback that is provided to the patient may comprise a few short bursts of vibration provided every half hour, a slight vibration two or three times a day, etc. In some versions, only one threshold value is provided (e.g., either an upper threshold to trigger vibratory alert when exceeded or a lower threshold to trigger vibratory alert when fallen below).

As noted above, port 1100 may be secured within patient by swiveling fasteners 10, with fasteners 10 being swiveled to the extended/deployed position upon rotation of actuator 12. As also noted above, ribs 48 a, 48 b and ribs 46 b of port 1100 provide a detent system that provides resistance to inadvertent rotation of actuator 12, thereby providing resistance to inadvertent retraction of swiveling fasteners 10. It should also be understood that this detent system may also provide resistance to inadvertent rotation of actuator 12 that might otherwise be caused by vibration of vibration generator 1210. Of course, a variety of other structures, components, features, or configurations may be used to prevent or resist inadvertent rotation of actuator 12 that might otherwise be caused by vibration of vibration generator 1210. Furthermore, port 1100 might lack swiveling fasteners 10 and might be secured within the patient in some other fashion. By way of example only, port 1100 may be secured within the patient using sutures, tacks, staples, biosurgical adhesive, and/or using any other suitable components, devices, or techniques, including combinations thereof.

In some settings, it may be desirable to deactivate vibration generator 1210 until port 1100 has been implanted in the patient. In other words, it may be desirable in some settings to prevent vibration generator 1210 from vibrating before and during the process of installing port 1100 in the patient. Otherwise, pressing of actuator 12 during the process of installing port 1100 in the patient might activate interface ring 1202 and thereby cause vibration generator 1210 to vibrate. There are a variety of ways in which vibration generator 1210 may be disabled before installation of port 1100 is complete. For instance, one or more bosses or other types of mechanical lockout feature may prevent actuator 12 from being moved downwardly toward port body 8 until after actuator 12 has been rotated to deploy fasteners 10 to the extended position. As another merely illustrative example, actuator 12 and/or interface ring 1202 may be configured such that downward movement of actuator 12 does not engage interface ring 1202 until after actuator 12 has been rotated to deploy fasteners 10 to the extended position. As yet another merely illustrative example, port 1100 may include a switch or other feature that enables interface ring 1202, with such a switch or other feature being engaged by actuator 12 after actuator 12 has been rotated to deploy fasteners 10 to the extended position. Still other suitable ways in which rotation of actuator 12 to the fastener 10 deploying position may be required in order to enable vibration of vibration generator 1210 will be apparent to those of ordinary skill in the art in view of the teachings herein.

As yet another variation, port 1100 may be configured such that vibration generator 1210 is unable to vibrate (even if actuator 12 is pressed downward) until after an initial enabling signal has been transmitted from an external coil to coil 1214 of port 1100. In other words, processor 1204 may include a logic that requires coil 1214 to first receive an unlocking signal or enablement signal before processor 1204 will command vibration generator 1210 to vibrate in response to actuator 12 being pressed downward. A physician may provide such an unlocking signal or enablement signal after port 1100 has been installed in the patient. Vibration generator 1210 may then be enabled to vibrate in response to downward pressing on actuator 12, even if such an external unlocking signal or enablement signal is no longer being transmitted to coil 1214. In a relatively simpler version, port 1100 may simply include a switch on its exterior that the physician may manipulate in order to make vibration generator 1210 responsive to downward pressing on actuator 12. Still various other suitable ways in which responsiveness of vibration generator 1210 may be selectively enabled and/or disabled will be apparent to those of ordinary skill in the art in view of the teachings herein.

While interface ring 1202 and interface sensor 1206 both “share” a common vibration generator 1210 and processor 1204 in the present example, it should be understood that interface ring 1202 and interface sensor 1206 may alternatively each have their own dedicated vibration generator 1210 and/or processor 1204. Accordingly, the inventors contemplate that the components shown in FIG. 31 may alternatively be provided in various other suitable numbers and/or arrangements. Furthermore, each of the components shown in FIG. 31 is merely optional.

It should be understood from the foregoing that vibration generators 1210 may be incorporated into virtually any type of implanted device. The above described examples of gastric band systems are mere illustrations. The inventors' contemplation is not limited to components of gastric band systems. By way of example only, a vibration generator 1210 may be incorporated into an implanted drug infusion port, chemotherapy port, or any other type of implantable port that is used to deliver medication, to help a physician locate the implanted port through palpation of the patient. Still other types of implanted devices that may incorporate a vibration generator 1210 will be apparent to those of ordinary skill in the art in view of the teachings herein. Likewise, any other teachings herein (e.g., relating to fasteners 10, etc.) may be incorporated into other devices and systems, and are certainly not limited to injection ports or gastric band systems.

Other suitable components, features, and operabilities that may be incorporated into port 2, 1100 are disclosed in U.S. patent application Ser. No. 12/640,048, filed Dec. 17, 2009, entitled “Implantable Port with Vibratory Feedback,” the disclosure of which is incorporated by reference herein. Still other suitable components, features, and operabilities that may be incorporated into port 2, 1100 will be apparent to those of ordinary skill in the art in view of the teachings herein.

In summary, numerous benefits have been described which result from employing the concepts of the invention. The foregoing description of one or more embodiments of the invention has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed. Modifications or variations are possible in light of the above teachings. The one or more embodiments were chosen and described in order to illustrate the principles of the invention and its practical application to thereby enable one of ordinary skill in the art to utilize the invention in various embodiments and with various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the claims submitted herewith. 

1. An injection port applier, wherein the injection port applier is configured to engage an injection port having integral fasteners that are movable from a non-deployed position to a deployed position, the injection port applier comprising: (a) a shaft having a proximal end and a distal end; (b) a port engagement portion at the distal end of the shaft, wherein the port engagement portion is configured to engage an injection port, wherein the port engagement portion comprises a fastener deployment member operable to move the fasteners of the injection port from the non-deployed position to the deployed position; and (c) a handle at the proximal end of the shaft, wherein the handle includes: (i) a first handle portion integral with the shaft, and (ii) a second handle portion movable relative to the first handle portion, wherein the second handle portion is movable distally, toward the first handle portion, to actuate the fastener deployment member to move the fasteners of the injection port from the non-deployed position to the deployed position.
 2. The injection port applier of claim 1, wherein at least part of the first handle portion extends transversely from the shaft.
 3. The injection port applier of claim 1, wherein at least part of the second handle portion extends transversely relative to the shaft.
 4. The injection port applier of claim 1, further comprising an elongate actuating member coupled with the second handle portion, wherein the elongate actuating member is in communication with the fastener deployment member, wherein the elongate actuating member is movable along a longitudinal axis defined by the elongate actuating member.
 5. The injection port applier of claim 4, wherein the elongate actuating member extends through at least part of the shaft.
 6. The injection port applier of claim 4, further comprising a cam pin and a cam ground, wherein the cam pin extends transversely from the elongate actuating member, wherein the cam pin is configured and positioned to engage the cam ground.
 7. The injection port applier of claim 6, wherein the cam ground defines a track, wherein the cam pin is disposed in the track.
 8. The injection port applier of claim 7, wherein the track is curved.
 9. The injection port applier of claim 6, wherein the cam ground comprises a cam collar, wherein the elongate actuating member extends through the cam collar, such that the cam collar is disposed about the elongate actuating member.
 10. The injection port applier of claim 6, wherein the cam ground and the cam pin are configured to cooperate to rotate at least part of the elongate actuating member about the longitudinal axis of the elongate actuating member as the elongate actuating member is moved along the longitudinal axis of the elongate actuating member.
 11. The injection port applier of claim 10, wherein the fastener deployment member is rotatable from a first position to a second position to move the fasteners of the injection port from the non-deployed position to the deployed position, wherein at least part of the elongate actuating member is operable to rotate the fastener deployment member in response to the cam pin and cam ground rotating at least part of the elongate actuating member.
 12. The injection port applier of claim 4, wherein the elongate actuating member has a bent flexible portion, wherein the flexible portion is configured to rotate while bent in order to rotate the fastener deployment member.
 13. The injection port applier of claim 1, further comprising a resilient member, wherein the resilient member is configured to bias the second handle portion proximally, away from the first handle portion.
 14. The injection port applier of claim 1, wherein the first handle portion is pivotally coupled with the second handle portion.
 15. An injection port applier, wherein the injection port applier is configured to engage an injection port having integral fasteners that are movable from a non-deployed position to a deployed position, the injection port applier comprising: (a) an elongate body having a proximal end and a distal end; (b) an actuating shaft assembly extending through at least a portion of the elongate body; (c) a port engagement portion at the distal end of the elongate body, wherein the port engagement portion is configured to engage an injection port, wherein the port engagement portion comprises a port actuator operable to move the fasteners of the injection port from the non-deployed position to the deployed position, wherein the actuating shaft assembly is movable relative to the elongate body in order to move the port actuator to thereby move the fasteners of the injection port from the non-deployed position to the deployed position; and (d) a handle at the proximal end of the elongate body, wherein the handle comprises: (i) a first handle portion in a fixed relationship with the elongate body, and (ii) a second handle portion movable relative to the first handle portion, wherein the second handle portion is coupled with the actuating shaft assembly, wherein the second handle portion is movable distally, toward the first handle portion, to move at least part of the actuating shaft assembly relative to the elongate body.
 16. The injection port applier of claim 15, wherein a first portion of the shaft assembly is configured to translate longitudinally relative to the elongate body, wherein a second portion of the shaft assembly is configured to rotate relative to the elongate body.
 17. The injection port applier of claim 16, further comprising a cam feature, wherein the cam feature is configured to rotate the second portion of the shaft assembly in response to translation of the first portion of the shaft assembly.
 18. The injection port applier of claim 15, wherein the port actuator is rotatable to move the fasteners of the injection port from the non-deployed position to the deployed position, wherein the shaft assembly is configured to rotate the port actuator in response to distal movement of the second handle portion.
 19. A method of using an injection port applier to install an injection port in a patient, wherein the injection port has a plurality of fasteners, wherein the injection port is removably coupled with the injection port applier, wherein the injection port applier comprises a fixed handle and an actuation handle, wherein the actuation handle is movable relative to the fixed handle, wherein the actuation handle is operable to move the fasteners from a non-deployed position to a deployed position, the method comprising: (a) positioning the injection port adjacent to tissue at a deployment site in a patient; and (b) pushing the actuation handle downwardly toward the patient in order to deploy the fasteners in the tissue, wherein the act of pushing the actuation handle downwardly comprises moving the actuation handle downwardly relative to the fixed handle.
 20. The method of claim 19, wherein the injection port applier further comprises a rotary actuator in communication with the actuation handle, wherein the actuation handle is operable to rotate the rotary actuator to move the fasteners from the non-deployed position to the deployed position, wherein the act of pushing the actuation handle downwardly toward the patient further comprises rotating the rotary actuator to move the fasteners from the non-deployed position to the deployed position. 